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Comparison of Surgical Outcomes of Craniotomy and Craniectomy in Posterior Fossa Lesions

Comparison Between Surgical Outcomes of Craniotomy and Craniectomy Among Patients with Posterior Fossa Lesion

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06831695
Enrollment
80
Registered
2025-02-18
Start date
2025-03-04
Completion date
2026-03-31
Last updated
2025-02-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Posterior Fossa Lesion

Keywords

Craniotomy, Craniectomy, Neurosurgery, Posterior Fossa, Brain Tumors

Brief summary

The purpose of this randomized controlled trial is to compare the surgical outcomes of craniotomy and craniectomy among patients with posterior fossa lesions. The study aims to determine differences in post-operative complications, hospital stay duration, and patient recovery between the two surgical techniques.

Detailed description

Patients diagnosed with posterior fossa lesions will be randomly assigned into two groups. Group A will undergo craniotomy, where the bone flap is replaced after dural closure, while Group B will undergo craniectomy, where the bone is permanently removed. Outcomes will be assessed based on post-operative complications such as CSF leakage, pseudomeningocele formation, post-operative headache, and length of hospital stay. The study aims to provide evidence to determine the superior surgical approach in terms of patient outcomes and healthcare cost reduction.

Interventions

PROCEDURECraniotomy

Intervention: Bone flap replaced after dural closure Additional Information: This procedure involves creating a single free bone flap using high-speed drills. The bone is repositioned and secured using mini plates or sutures after the surgical intervention is completed. Post-operative monitoring will include assessment for CSF leakage, wound healing, and neurological recovery.

PROCEDURECraniectomy

Intervention: Bone permanently removed Additional Information: In this approach, the bone is removed in pieces using rongeurs, leaving an open dural surface without replacement of the bone. The dura is closed with sutures, and dural augmentation may be performed as needed. Post-operative assessment will focus on complications such as pseudomeningocele, CSF leakage, and extended hospital stays.

Sponsors

University of Health Sciences Lahore
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
7 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* Patients diagnosed with posterior fossa lesions * Age range: 7-70 years * Patients with cerebellar hematoma (traumatic or spontaneous)

Exclusion criteria

* Previous posterior fossa surgery * Brainstem hematoma * Tumors involving the overlying dura or bone

Design outcomes

Primary

MeasureTime frameDescription
Incidence of CSF leakageUp to 6 months post-surgeryDefinition: CSF leakage is defined as the presence of clear fluid discharge from the surgical site, confirmed via clinical examination and biochemical analysis of β-2 transferrin. Measurement: Evaluated by clinical assessment at routine follow-ups and imaging studies when indicated.
Occurrence of pseudomeningoceleUp to 6 months post-surgeryDefinition: Pseudomeningocele is defined as an abnormal collection of cerebrospinal fluid in the surgical site, detected through physical examination and confirmed by imaging techniques such as MRI or CT scan. Measurement: Follow-up visits at 1, 3, and 6 months post-surgery.
Severity of post-operative headacheImmediately post-surgery, at 3 months, and at 6 months post-surgeryDefinition: Post-operative headache will be assessed using the Catalano grading system, categorizing severity from 0 (no headache) to 4 (severe, refractory to medication). Measurement: Self-reported patient evaluations at each follow-up visit.
Length of hospital stayFrom immediate post-surgery until hospital discharge, assessed up to 4 weeksDefinition: The total number of days a patient remains hospitalized post-surgery, including any extended stay due to complications. Measurement: Recorded from hospital admission to discharge.

Contacts

Primary ContactDr. Birat Thapa Magar, Post Graduate Resident
biratjmagar.5@gmail.com+923057895437

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026